Jóźwiak S, Orzeszko E, Michałowicz R, Woźniewicz B
Zespół Neurologii Dzieciecej Centrum Zdrowia Dziecka w Warszawie.
Pediatr Pol. 1995 Jan;70(1):71-4.
Three children with a diagnosis of congenital muscular dystrophy are described. Because of the heterogeneity of these disorders the authors stress the necessity of differentiation with other causes of "floppy infant" syndrome, especially with Werdnig-Hoffmann disease, structural myopathies, and Duchenne progressive muscular dystrophy. An extensive hypodense area on brain CT scan was found in one child.
本文描述了三名被诊断为先天性肌营养不良的儿童。由于这些疾病的异质性，作者强调了与“松软婴儿”综合征的其他病因进行鉴别诊断的必要性，尤其是与韦尼克-霍夫曼病、结构性肌病和杜兴氏进行性肌营养不良症相鉴别。在一名儿童的脑部CT扫描中发现了广泛的低密度区域。
